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Different Covalent Immobilizations Modulate Lipase Activities of Hypocrea pseudokoningii
Enzyme immobilization can promote several advantages for their industrial application. In this work, a lipase from Hypocrea pseudokoningii was efficiently linked to four chemical supports: agarose activated with cyanogen bromide (CNBr), glyoxyl-agarose (GX), MANAE-agarose activated with glutaraldehy...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151390/ https://www.ncbi.nlm.nih.gov/pubmed/28869529 http://dx.doi.org/10.3390/molecules22091448 |
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author | Pereira, Marita G. Velasco-Lozano, Susana Moreno-Perez, Sonia Polizeli, Aline M. Heinen, Paulo R. Facchini, Fernanda D. A. Vici, Ana C. Cereia, Mariana Pessela, Benevides C. Fernandez-Lorente, Gloria Guisan, Jose M. Jorge, João A. Polizeli, Maria de Lourdes T. M. |
author_facet | Pereira, Marita G. Velasco-Lozano, Susana Moreno-Perez, Sonia Polizeli, Aline M. Heinen, Paulo R. Facchini, Fernanda D. A. Vici, Ana C. Cereia, Mariana Pessela, Benevides C. Fernandez-Lorente, Gloria Guisan, Jose M. Jorge, João A. Polizeli, Maria de Lourdes T. M. |
author_sort | Pereira, Marita G. |
collection | PubMed |
description | Enzyme immobilization can promote several advantages for their industrial application. In this work, a lipase from Hypocrea pseudokoningii was efficiently linked to four chemical supports: agarose activated with cyanogen bromide (CNBr), glyoxyl-agarose (GX), MANAE-agarose activated with glutaraldehyde (GA) and GA-crosslinked with glutaraldehyde. Results showed a more stable lipase with both the GA-crosslinked and GA derivatives, compared to the control (CNBr), at 50 °C, 60 °C and 70 °C. Moreover, all derivatives were stabilized when incubated with organic solvents at 50%, such as ethanol, methanol, n-propanol and cyclohexane. Furthermore, lipase was highly activated (4-fold) in the presence of cyclohexane. GA-crosslinked and GA derivatives were more stable than the CNBr one in the presence of organic solvents. All derivatives were able to hydrolyze sardine, açaí (Euterpe oleracea), cotton seed and grape seed oils. However, during the hydrolysis of sardine oil, GX derivative showed to be 2.3-fold more selectivity (eicosapentaenoic acid (EPA)/docosahexaenoic acid (DHA) ratio) than the control. Additionally, the types of immobilization interfered with the lipase enantiomeric preference. Unlike the control, the other three derivatives preferably hydrolyzed the R-isomer of 2-hydroxy-4-phenylbutanoic acid ethyl ester and the S-isomer of 1-phenylethanol acetate racemic mixtures. On the other hand, GX and CNBr derivatives preferably hydrolyzed the S-isomer of butyryl-2-phenylacetic acid racemic mixture while the GA and GA-crosslink derivatives preferably hydrolyzed the R-isomer. However, all derivatives, including the control, preferably hydrolyzed the methyl mandelate S-isomer. Moreover, the derivatives could be used for eight consecutive cycles retaining more than 50% of their residual activity. This work shows the importance of immobilization as a tool to increase the lipase stability to temperature and organic solvents, thus enabling the possibility of their application at large scale processes. |
format | Online Article Text |
id | pubmed-6151390 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-61513902018-11-13 Different Covalent Immobilizations Modulate Lipase Activities of Hypocrea pseudokoningii Pereira, Marita G. Velasco-Lozano, Susana Moreno-Perez, Sonia Polizeli, Aline M. Heinen, Paulo R. Facchini, Fernanda D. A. Vici, Ana C. Cereia, Mariana Pessela, Benevides C. Fernandez-Lorente, Gloria Guisan, Jose M. Jorge, João A. Polizeli, Maria de Lourdes T. M. Molecules Article Enzyme immobilization can promote several advantages for their industrial application. In this work, a lipase from Hypocrea pseudokoningii was efficiently linked to four chemical supports: agarose activated with cyanogen bromide (CNBr), glyoxyl-agarose (GX), MANAE-agarose activated with glutaraldehyde (GA) and GA-crosslinked with glutaraldehyde. Results showed a more stable lipase with both the GA-crosslinked and GA derivatives, compared to the control (CNBr), at 50 °C, 60 °C and 70 °C. Moreover, all derivatives were stabilized when incubated with organic solvents at 50%, such as ethanol, methanol, n-propanol and cyclohexane. Furthermore, lipase was highly activated (4-fold) in the presence of cyclohexane. GA-crosslinked and GA derivatives were more stable than the CNBr one in the presence of organic solvents. All derivatives were able to hydrolyze sardine, açaí (Euterpe oleracea), cotton seed and grape seed oils. However, during the hydrolysis of sardine oil, GX derivative showed to be 2.3-fold more selectivity (eicosapentaenoic acid (EPA)/docosahexaenoic acid (DHA) ratio) than the control. Additionally, the types of immobilization interfered with the lipase enantiomeric preference. Unlike the control, the other three derivatives preferably hydrolyzed the R-isomer of 2-hydroxy-4-phenylbutanoic acid ethyl ester and the S-isomer of 1-phenylethanol acetate racemic mixtures. On the other hand, GX and CNBr derivatives preferably hydrolyzed the S-isomer of butyryl-2-phenylacetic acid racemic mixture while the GA and GA-crosslink derivatives preferably hydrolyzed the R-isomer. However, all derivatives, including the control, preferably hydrolyzed the methyl mandelate S-isomer. Moreover, the derivatives could be used for eight consecutive cycles retaining more than 50% of their residual activity. This work shows the importance of immobilization as a tool to increase the lipase stability to temperature and organic solvents, thus enabling the possibility of their application at large scale processes. MDPI 2017-09-04 /pmc/articles/PMC6151390/ /pubmed/28869529 http://dx.doi.org/10.3390/molecules22091448 Text en © 2017 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Pereira, Marita G. Velasco-Lozano, Susana Moreno-Perez, Sonia Polizeli, Aline M. Heinen, Paulo R. Facchini, Fernanda D. A. Vici, Ana C. Cereia, Mariana Pessela, Benevides C. Fernandez-Lorente, Gloria Guisan, Jose M. Jorge, João A. Polizeli, Maria de Lourdes T. M. Different Covalent Immobilizations Modulate Lipase Activities of Hypocrea pseudokoningii |
title | Different Covalent Immobilizations Modulate Lipase Activities of Hypocrea pseudokoningii |
title_full | Different Covalent Immobilizations Modulate Lipase Activities of Hypocrea pseudokoningii |
title_fullStr | Different Covalent Immobilizations Modulate Lipase Activities of Hypocrea pseudokoningii |
title_full_unstemmed | Different Covalent Immobilizations Modulate Lipase Activities of Hypocrea pseudokoningii |
title_short | Different Covalent Immobilizations Modulate Lipase Activities of Hypocrea pseudokoningii |
title_sort | different covalent immobilizations modulate lipase activities of hypocrea pseudokoningii |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6151390/ https://www.ncbi.nlm.nih.gov/pubmed/28869529 http://dx.doi.org/10.3390/molecules22091448 |
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